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Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence. (Q45289187)

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scientific article published in August 1994

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English	Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence.	scientific article published in August 1994

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29 October 2019

Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951324%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Huntington's disease

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1 reference

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inferred from title

Rajkumar Ramesar

5

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Europe PubMed Central

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29 October 2019

9

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29 October 2019

7

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29 October 2019

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Rubinsztein DC

1

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29 October 2019

Amos W

2

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29 October 2019

Leggo J

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29 October 2019

Goodburn S

4

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29 October 2019

Old J

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29 October 2019

McMahon R

8

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29 October 2019

Ferguson-Smith MA

10

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29 October 2019

publication date

1 August 1994

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29 October 2019

language of work or name

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Nature Genetics

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951324%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

7

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Europe PubMed Central

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29 October 2019

4

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Europe PubMed Central

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29 October 2019

525-530

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951324%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Trinucleotide repeat length instability and age of onset in Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

21 January 2018

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

21 January 2018

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

21 January 2018

Site of (CCG) polymorphism in the HD gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

21 January 2018

A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

21 January 2018

Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

21 January 2018

De novo expansion of a (CAG)n repeat in sporadic Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

21 January 2018

Triplet repeat genes raise questions

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

21 January 2018

Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

21 January 2018

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

7 January 2021

based on heuristic

inferred from DOI database lookup

A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat number

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

7 January 2021

based on heuristic

inferred from DOI database lookup

The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

7 January 2021

based on heuristic

inferred from DOI database lookup

Meiotic drive at the myotonic dystrophy locus?

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

7 January 2021

based on heuristic

inferred from DOI database lookup

Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-525

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/NG0894-525

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951324%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Dimensions publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

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29 October 2019

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